CATEGORIES: Applied Therapeutics | CMT Type - SORD Deficiency | CMT-Connect | CMT-Connect Webinars | Featured

SORD Webinar – Part 2 – Clinical Trial Update

by Courtney | Oct 9, 2022 | 0 comments

Learn more on this topic

CMT Research: Got a Birthday Coming up?

by Courtney | May 26, 2026 | Featured, Ways to Give | 0 Comments

CMT Research: Got a Birthday Coming up? If your birthday falls between June and August, this...

HNF to Host FDA Patient Listening Session for CMT-SORD

by Courtney | May 21, 2026 | CMT Type - SORD Deficiency | 0 Comments

HNF to Host FDA Patient Listening Session for CMT-SORD The Hereditary Neuropathy Foundation is...

Thank You for an Incredible 2026 CMT Clinical Trial Readiness Summit

by Courtney | May 21, 2026 | CMT Summit, Community, Featured, Living with CMT, Past Events | 0 Comments

Thank you for being part of our 2026 CMT Summit, our biggest gathering yet, with over 200...

Your Genetic Report Could Help Unlock the Next CMT Breakthrough

by Courtney | May 21, 2026 | CMT Type - CMT1A, CMT Type - CMT1B, CMT Type - CMT1X, CMT Type - CMT2A, CMT Type - CMT2C, CMT Type - CMT4A GDAP1, CMT Type - HNPP, CMT Type - SORD Deficiency, GRIN Patient Registry | 0 Comments

Your Genetic Report Could Help Unlock the Next CMT Breakthrough You may not be a scientist. But...

The 2026 CMT Summit: What We Built Together

by Courtney | May 18, 2026 | CMT Summit, Featured, Living with CMT, Newly Diagnosed, Our Impact, Past Events, Patient-Focused Research | 0 Comments

The 2026 CMT Summit: What We Built Together Two days. One community that keeps growing. The...

HNF Driving Progress at the 2026 MDA Clinical & Scientific Conference

by Courtney | Mar 17, 2026 | Advocacy, Awareness, Featured, GRIN Patient Registry, Living with CMT, Our Impact, TRIAD - Clinical Trial Readiness | 0 Comments

HNF Driving Progress at the 2026 MDA Clinical & Scientific Conference The Hereditary...

Webinar Recording: Why CMT Biomarkers Can’t Wait

by Courtney | Feb 6, 2026 | Featured, Research, Research and Critical Trials, Webinars - Research and Clinical Trials | 0 Comments

Webinar Recording: Why CMT Biomarkers Can’t Wait Thank you to everyone who joined HNF’s live...

Allison Moore Receives Award for Community Impact in Research

by Courtney | Jan 14, 2026 | Advocacy, Awareness, Featured, Gene Therapy, GRIN Patient Registry, Living with CMT, Research, Research and Critical Trials, TRIAD | 0 Comments

Muscular Dystrophy Association’s Legacy Awards Honor Innovators in Clinical and Scientific...

Biomarkers Can’t Wait

by Courtney | Dec 12, 2025 | Research, Webinars - Research and Clinical Trials | 0 Comments

Webinar Announcement: Biomarkers Can’t Wait – Accelerating the Path to CMT Treatments Biomarkers...

HNF Partners with MDA to Empower the CMT Community

by Courtney | Oct 13, 2025 | Community, Featured, Living with CMT, Webinars - Bracing, Webinars - Newly Diagnosed, Webinars - Research and Clinical Trials | 0 Comments

HNF Partners with MDA for CMT Series The Hereditary Neuropathy Foundation (HNF) was honored to...

WHAT IS CMT

TYPES OF CMT

PATIENT RESOURCES

CMT UPDATES

CMT CONNECT

CMT Research

TRIAD

GRIN PATIENT REGISTRY

PEDIATRICS & CMT

WHAT IS MITO

TYPES OF MITOS

MITO Faces

MITO Research

TRIAD - Mito

GRIN PATIENT REGISTRY

PEDIATRICS & MITO CMT

FDA

CLINICAL TRIALS

PATIENT-FOCUSED RESEARCH

EMERGING TECHNOLOGIES

GENETIC TESTING - CMT GENIE

MOVEMENT IS MEDICINE™

FACES OF CMT

INDUSTRY

HCPs/CENTERS OF EXCELLENCE

RESEARCH FUNDING

About HNF

OUR STORY

FOUNDATION LEADERSHIP

990's & ANNUAL REPORTS

Join Team CMT

Ways to Give

Amazon Wishlist

CMT Shop

GRIN Registry

Facebook Fundraiser

Celebrate your birthday with a purpose

Participate or Host an event

SORD Webinar – Part 2 – Clinical Trial Update

Learn more on this topic

Related Blog Posts

Join the conversation

Leave a Comment

0 Comments

Submit a Comment Cancel reply

Newsletter

Join for notifications on events, campaigns, & news

Success!